ClinVar Miner

Submissions for variant NM_172240.3(POC1B):c.1185C>T (p.Ser395=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005011707 SCV005632092 uncertain significance Cone-rod dystrophy 20 2024-02-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005112564 SCV005784050 likely benign not provided 2024-05-31 criteria provided, single submitter clinical testing

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